 Hemophilia A
"Hemophilia A" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.
| Descriptor ID |
D006467
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| MeSH Number(s) |
C15.378.100.100.500 C15.378.100.141.500 C15.378.463.500 C16.320.099.500
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| Concept/Terms |
Hemophilia A- Hemophilia A
- Hemophilia As
- Haemophilia
- Hemophilia A, Congenital
- Congenital Hemophilia A
- Congenital Hemophilia As
- Hemophilia As, Congenital
- Hemophilia, Classic
- Classic Hemophilia
- Classic Hemophilias
- Hemophilias, Classic
- Hemophilia
Autosomal Hemophilia A- Autosomal Hemophilia A
- As, Autosomal Hemophilia
- Autosomal Hemophilia As
- Hemophilia A, Autosomal
- Hemophilia As, Autosomal
Factor VIII Deficiency- Factor VIII Deficiency
- Factor 8 Deficiency, Congenital
- Factor VIII Deficiency, Congenital
- Deficiency, Factor VIII
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Below are MeSH descriptors whose meaning is more general than "Hemophilia A".
Below are MeSH descriptors whose meaning is more specific than "Hemophilia A".
This graph shows the total number of publications written about "Hemophilia A" by people in UAMS Profiles by year, and whether "Hemophilia A" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2024 | 2 | 0 | 2 | | 2022 | 2 | 0 | 2 | | 2019 | 1 | 0 | 1 | | 2013 | 2 | 0 | 2 | | 2011 | 1 | 0 | 1 | | 2009 | 1 | 0 | 1 | | 2007 | 1 | 0 | 1 | | 2006 | 1 | 0 | 1 | | 2004 | 1 | 0 | 1 | | 1991 | 1 | 0 | 1 | | 1989 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hemophilia A" by people in Profiles over the past ten years.
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Appell LE, Mack JM, Farrar JE, Roper SN, Savage MR, Pandey S, Crary SE. Acquired Hemophilia: A Rare Complication of Pediatric Idiopathic Multicentric Castleman Disease. Pediatrics. 2024 Apr 01; 153(4).
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Leavitt AD, Konkle BA, Stine KC, Visweshwar N, Harrington TJ, Giermasz A, Arkin S, Fang A, Plonski F, Yver A, Ganne F, Agathon D, Resa MLA, Tseng LJ, Di Russo G, Cockroft BM, Cao L, Rupon J. Giroctocogene fitelparvovec gene therapy for severe hemophilia A: 104-week analysis of the phase 1/2 Alta?study. Blood. 2024 02 29; 143(9):796-806.
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Sidarous GK, Roy AM, Sasapu A. Acquired Hemophilia A in a Patient With Multiple Sclerosis. Perm J. 2022 06 29; 26(2):153-157.
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Citla-Sridhar D, Sidonio RF, Ahuja SP. Bone health in haemophilia carriers and persons with von Willebrand disease: A large database analysis. Haemophilia. 2022 Jul; 28(4):671-678.
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Gourishankar A, C. Sridhar D, Rodriquez N. Acute Swollen Calf Pain With a Diagnosis of Hemophilia Following an MRI. J Pediatr Hematol Oncol. 2019 10; 41(7):559-560.
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Ferraris VA, Boral LI, Cohen AJ, Smyth SS, White GC. Consensus review of the treatment of cardiovascular disease in people with hemophilia A and B. Cardiol Rev. 2015 Mar-Apr; 23(2):53-68.
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